Canonical Allele Identifier: CA359802471

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155617C>G (hg19) ; chr5:g.56859790C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859790C>G , CM000667.2:g.56859790C>G	GRCh38
NC_000005.9:g.56155617C>G , CM000667.1:g.56155617C>G	GRCh37
NC_000005.8:g.56191374C>G	NCBI36
NG_031884.1:g.49718C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.709C>G MANE Select	ENSP00000382423.3:p.Gln237Glu
ENST00000399503.3:c.709C>G	ENSP00000382423.3:p.Gln237Glu
NM_005921.1:c.709C>G	NP_005912.1:p.Gln237Glu
XM_005248519.3:c.331C>G	XP_005248576.2:p.Gln111Glu
XM_011543406.1:c.454C>G	XP_011541708.1:p.Gln152Glu
XM_011543407.1:c.709C>G	XP_011541709.1:p.Gln237Glu
XM_011543408.1:c.709C>G	XP_011541710.1:p.Gln237Glu
XM_017009484.1:c.298C>G	XP_016864973.1:p.Gln100Glu
XM_017009485.1:c.220C>G	XP_016864974.1:p.Gln74Glu
XR_001742068.2:n.740C>G
NM_005921.2:c.709C>G MANE Select	NP_005912.1:p.Gln237Glu